JPH0261082B2 - - Google Patents
Info
- Publication number
- JPH0261082B2 JPH0261082B2 JP59199099A JP19909984A JPH0261082B2 JP H0261082 B2 JPH0261082 B2 JP H0261082B2 JP 59199099 A JP59199099 A JP 59199099A JP 19909984 A JP19909984 A JP 19909984A JP H0261082 B2 JPH0261082 B2 JP H0261082B2
- Authority
- JP
- Japan
- Prior art keywords
- alumina
- dielectric constant
- weight
- catio
- porcelain
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 12
- 229910052573 porcelain Inorganic materials 0.000 claims description 8
- 239000000203 mixture Substances 0.000 claims description 7
- 229910002971 CaTiO3 Inorganic materials 0.000 claims 1
- 229910052593 corundum Inorganic materials 0.000 claims 1
- 229910001845 yogo sapphire Inorganic materials 0.000 claims 1
- WEUCVIBPSSMHJG-UHFFFAOYSA-N calcium titanate Chemical compound [O-2].[O-2].[O-2].[Ca+2].[Ti+4] WEUCVIBPSSMHJG-UHFFFAOYSA-N 0.000 description 6
- 229910010413 TiO 2 Inorganic materials 0.000 description 5
- 239000013065 commercial product Substances 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 229910018072 Al 2 O 3 Inorganic materials 0.000 description 3
- 239000003153 chemical reaction reagent Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 229910002367 SrTiO Inorganic materials 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- -1 polyethylene Polymers 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 238000001694 spray drying Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 229910006404 SnO 2 Inorganic materials 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000001354 calcination Methods 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 229910010293 ceramic material Inorganic materials 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 239000003989 dielectric material Substances 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 238000005469 granulation Methods 0.000 description 1
- 230000003179 granulation Effects 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/01—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics
- C04B35/10—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on aluminium oxide
- C04B35/111—Fine ceramics
Landscapes
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Ceramic Engineering (AREA)
- Manufacturing & Machinery (AREA)
- Materials Engineering (AREA)
- Structural Engineering (AREA)
- Organic Chemistry (AREA)
- Inorganic Insulating Materials (AREA)
- Compositions Of Oxide Ceramics (AREA)
Description
「産業上の利用分野」
本発明は、マイクロ波領域、特にX−band以
上の周波数領域において使用されるもので、これ
ら高周波領域で高い無負荷Qと、低い比誘電率を
呈するアルミナ磁器組成物を提供しようとするも
のである。
「従来技術」
従来、誘電体磁器材料として、ZrO2−SnO2−
TiO2系BaO−TiO2系磁器及びその一部を他の元
素で置換した磁器、あるいは比誘電率の温度係数
が正の値を示す誘電体磁器又はガラスと、負の値
を示すTiO2を組合わせて温度係数を制御しよう
としたものが知られているが、これらの材料は比
誘電率が30〜40と高かつた。
一方、使用周波数が高くなるに従い、誘電体共
振器用磁器としては加工性の面から比誘電率が小
さい材料が要望されるようになつた。
かかる比誘電率の小さい材料としてアルミナ磁
器が注目されている。アルミナ磁器の比誘電率は
10程度のものが得られるが、共振周波数の温度係
数が−60ppm/℃と極めて大きかつた。
本出願人は、先に特願昭59−151589号(特開昭
61−32306号)において、Al2O3−CaTiO3−
SrTiO3三成分系組成図中、モル分率で打点した。
Al2O3 CaTiO3 SrTiO3
点A 0.99 0.01 0
点B 0.96 0.04 0
点C 0.91 0.04 0.05
点D 0.91 0.01 0.08
の点A,B,C及びDを逐次結んでなる4辺形区
域内の組成物で、共振周波数の温度係数(以下〓
fとする)において、上記の−60ppm/℃と絶対
値の大きい負の値を取り、無負荷Qが高く高周波
における誘電損失が小さく、しかも熱伝導性、機
械的強度、化学的安定性に富むアルミナ焼結体
と、CaOとTiO2とによつて生成され、上記の〓
fが+900に近い正の大きな値を示すチタン酸カ
ルシウム(CaTiO3)の少量とを複合させてなる
2成分系及びチタン酸ストロウムを加えて3成分
系の高周波誘電材料として優れたアルミナ磁器組
成物について提案した。
「発明が解決しようとする問題点」
上記の特願昭59−151589号の発明によつて得ら
れる無負荷Qを更に改善しようとするものであ
る。
「問題点を解決するための手段」
本発明は上記の特願昭59−151589号のアルミナ
焼結体と、チタン酸カルシウムをモル比で前者ア
ルミナ96〜99.5%、チタン酸カルシウム4〜0.5
%に規定してなる2成分系を主体とすると共に両
者の複合体100重量部に対し、MgOを1重量部以
下の割合で含有させることによつて、特に無負荷
Qを高め、かつ比較電率を低下させようとするの
である。
「作用」
上記のMgOが無負荷Qを高め、比誘電率を低
下させる。
「実施例」
(1) チタン酸カルシウムの合成
炭酸カルシウム(CaCO3市販品・試薬特級)
555g
二酸化チタン(TiO2市販品・試薬特級) 445g
水 1500ml
をアルミナ球石(純度99.99%・20mmφ)2Kg
と共に2のポリエチレン容器を用い、
84RPM・20時間の混合を行ない、乾燥後42メ
ツシユの篩通し後、純度99.99のアルミナルツ
ボに移し、電気炉にて1300℃・1時間の仮焼を
行なつてCaTiO3を合成、20メツシユの篩を通
した後、仮焼前に行なつた混合と同一条件の再
粉砕及び乾燥、篩通しによつて42メツシユ全通
のチタン酸カルシウムCaTiO3の粉末を得た。
(2) 調合
アルミナ(市販品・純度99.99%・平均粒径
0.5μ)950gに対し、最終生成物として上記の
合成したチタン酸カルシウムを第1表の各モル
比が得られるように配合し、更にこれらの配合
物100重量部に対してMgOとして同表に示すよ
う0〜1.2重量部の割合で含有させるよう炭酸
マグネシウム(MgCO3市販品・試薬特級)と
水1000mlを加え、アルミナ球石(純度99.99
%・20mmφ)2Kgと共に8のポリエチレン容
器に移し、60RPM・20時間の混合を行なつた
後、各混合物に有機質粘結剤としてポリビニル
アルコールの33%水溶液30gを加え、再び3時
間の混合を行なつてスラリー化し、これらのス
ラリーをガス温度180℃・アトマイザー100mm
φ・7200RPMの噴霧乾燥によつて造粒した。
噴霧乾燥によつて造粒された40〜150μの顆
粒粉末を1500Kg/cm2の金型プレスによつて19mm
φ×10.5mmLに成形、電気炉にて1400〜1450
℃・1時間保持の焼成を行ない、ついで15mmφ
×8mmLに研磨加工した。
仕上精度は両端部0.1S・外周面が0.5Sとし各
試料の無負荷Q・比誘電率εを測定した結果を
第1表に示す。
"Industrial Application Field" The present invention is used in the microwave region, particularly in the frequency region above the X-band, and is an alumina porcelain composition that exhibits a high no-load Q and a low dielectric constant in these high frequency regions. This is what we are trying to provide. “Prior art” Conventionally, ZrO 2 −SnO 2 − was used as a dielectric ceramic material.
TiO 2 -based BaO-TiO 2 -based porcelain, porcelain in which part of it has been replaced with other elements, or dielectric porcelain or glass with a positive temperature coefficient of dielectric constant, and TiO 2 with a negative value. It is known that attempts have been made to control the temperature coefficient by combining materials, but these materials have a high dielectric constant of 30 to 40. On the other hand, as the frequency of use increases, materials with a small dielectric constant are required for ceramics for dielectric resonators from the viewpoint of workability. Alumina porcelain is attracting attention as a material with such a low dielectric constant. The dielectric constant of alumina porcelain is
10, but the temperature coefficient of the resonant frequency was extremely large at -60 ppm/°C. The applicant previously filed Japanese Patent Application No. 59-151589 (Japanese Unexamined Patent Publication No.
61-32306), Al 2 O 3 −CaTiO 3 −
In the SrTiO 3 ternary composition diagram, the mole fractions are dotted. Al 2 O 3 CaTiO 3 SrTiO 3 points A 0.99 0.01 0 point B 0.96 0.04 0 point C 0.91 0.04 0.05 point D 0.91 0.01 0.08 Composition within a quadrilateral area formed by sequentially connecting points A, B, C, and D Then, the temperature coefficient of the resonant frequency (hereinafter 〓
f), it takes a negative value with a large absolute value of -60 ppm/℃, has a high no-load Q, and has low dielectric loss at high frequencies, and is rich in thermal conductivity, mechanical strength, and chemical stability. It is produced by alumina sintered body, CaO and TiO 2 , and the above
An alumina porcelain composition that is excellent as a high-frequency dielectric material in a two-component system made by combining it with a small amount of calcium titanate (CaTiO 3 ) having a large positive value of f close to +900, and in a three-component system by adding stroium titanate. I proposed about. ``Problems to be Solved by the Invention'' This invention attempts to further improve the no-load Q obtained by the invention of Japanese Patent Application No. 59-151589. "Means for Solving the Problems" The present invention consists of the alumina sintered body of the above-mentioned Japanese Patent Application No. 151589/1982 and calcium titanate in a molar ratio of 96 to 99.5% alumina and 4 to 0.5% calcium titanate.
%, and by containing MgO at a ratio of 1 part by weight or less per 100 parts by weight of the composite of both, the no-load Q can be particularly increased and the comparative voltage can be improved. The aim is to reduce the rate. "Effect" The above MgO increases the no-load Q and lowers the relative dielectric constant. "Example" (1) Synthesis of calcium titanate Calcium carbonate (CaCO 3 commercial product/reagent special grade)
555g titanium dioxide (TiO 2 commercial product, reagent grade) 445g water 1500ml and 2kg alumina coccule (purity 99.99%, 20mmφ)
and using 2 polyethylene containers,
Mixing was carried out at 84 RPM for 20 hours, and after drying, 42 meshes were passed through a sieve, transferred to an aluminum crucible with a purity of 99.99, and calcined in an electric furnace at 1300℃ for 1 hour to synthesize CaTiO 3 . After passing through a sieve, 42 meshes of calcium titanate CaTiO 3 powder were obtained by re-pulverizing, drying, and passing through a sieve under the same conditions as the mixing performed before calcination. (2) Mixed alumina (commercial product, purity 99.99%, average particle size
To 950 g of 0.5 μ), the above-synthesized calcium titanate was blended as the final product so as to obtain each molar ratio shown in Table 1, and further, to 100 parts by weight of these blends, the amount of MgO shown in the table was added. Add magnesium carbonate (MgCO 3 commercial product, special grade reagent) and 1000 ml of water to contain 0 to 1.2 parts by weight as shown, and add alumina coccule (purity 99.99).
%・20mmφ) 2Kg into a polyethylene container No. 8, and mixed at 60RPM for 20 hours. Added 30g of a 33% aqueous solution of polyvinyl alcohol as an organic binder to each mixture and mixed again for 3 hours. The slurry is heated to a gas temperature of 180℃ and an atomizer of 100mm.
Granulation was performed by spray drying at φ 7200 RPM. The 40-150μ granule powder granulated by spray drying is sized to 19mm by a 1500Kg/ cm2 mold press.
Formed into φ×10.5mmL, 1400~1450 in electric furnace
℃ for 1 hour, then 15mmφ
Polished to x8mmL. The finishing accuracy was 0.1S on both ends and 0.5S on the outer circumference, and the results of measuring the no-load Q and dielectric constant ε of each sample are shown in Table 1.
【表】【table】
【表】
測定方法
ε 誘電体円柱共振器法(共振周波数8GHz)
による。
「発明の効果」
第1表によつて明らかにされる通り、本発明の
Al2O3/CaTiO3のモル比が99.5/0.5〜96/4の
範囲内にあり、かつMgOを1.0外重量%以内で含
有する試料No.1〜5で、それぞれ副No.B〜Hの試
料はいずれも無負荷Q〜7000以上、比誘電率ε13
以下を呈し、マイクロ波領域、特にX−band以
上の周波数領域における使用に対して著効を奏す
る。[Table] Measurement method
ε Dielectric cylindrical resonator method (resonance frequency 8GHz)
by.
“Effects of the invention” As shown in Table 1, the effects of the invention
Samples Nos. 1 to 5 have a molar ratio of Al 2 O 3 /CaTiO 3 in the range of 99.5/0.5 to 96/4 and contain MgO within 1.0% by weight, and sub Nos. B to H, respectively. All samples have an unloaded Q of over 7000 and a relative dielectric constant of ε13.
It exhibits the following properties and is particularly effective for use in the microwave region, particularly in the frequency region above the X-band.
Claims (1)
からなる主成分100重量部に対して、副成分とし
てMgOを1重量部以下の割合で添加、含有させ
てなるアルミナ磁器組成物。1 Al2O3 96-99.5 mol%, CaTiO3 4-0.5 mol%
An alumina porcelain composition containing MgO as a subcomponent in a ratio of 1 part by weight or less to 100 parts by weight of the main component.
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP59199099A JPS6177208A (en) | 1984-09-22 | 1984-09-22 | Almina ceramic composition |
| US06/778,652 US4614725A (en) | 1984-09-22 | 1985-09-23 | Alumina porcelain composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP59199099A JPS6177208A (en) | 1984-09-22 | 1984-09-22 | Almina ceramic composition |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6177208A JPS6177208A (en) | 1986-04-19 |
| JPH0261082B2 true JPH0261082B2 (en) | 1990-12-19 |
Family
ID=16402103
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP59199099A Granted JPS6177208A (en) | 1984-09-22 | 1984-09-22 | Almina ceramic composition |
Country Status (2)
| Country | Link |
|---|---|
| US (1) | US4614725A (en) |
| JP (1) | JPS6177208A (en) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS61211907A (en) * | 1985-03-15 | 1986-09-20 | 日本特殊陶業株式会社 | Alumina ceramic composition |
| JPH07109725B2 (en) * | 1986-05-27 | 1995-11-22 | 株式会社村田製作所 | Dielectric porcelain composition |
| JPS6376206A (en) * | 1986-09-18 | 1988-04-06 | 日本特殊陶業株式会社 | Alumina ceramic composition |
| US5147835A (en) * | 1991-03-05 | 1992-09-15 | Motorola, Inc. | Composite titanate aluminate dielectric material |
| JP2625074B2 (en) * | 1992-06-24 | 1997-06-25 | 京セラ株式会社 | Dielectric ceramic composition and dielectric resonator |
| US5821181A (en) * | 1996-04-08 | 1998-10-13 | Motorola Inc. | Ceramic composition |
| EP1065190A3 (en) | 1999-06-29 | 2001-05-16 | Hitachi Metals, Ltd. | Alumina ceramic composition |
| AU1788201A (en) * | 1999-12-15 | 2001-06-25 | Koman, Ltd. | Ceramic material and method of obtaining same |
| DE10221866A1 (en) * | 2002-05-15 | 2003-11-27 | Marconi Comm Gmbh | Production of aluminum oxide ceramic used as a dielectric material comprises sintering a mixture consisting of an aluminum oxide powder and titanium-containing oxide powder, and calcining the body formed at a calcining temperature |
| US10246375B2 (en) | 2016-03-30 | 2019-04-02 | Skyworks Solutions, Inc. | Multi-phase high thermal conductivity composite dielectric materials |
| US12512232B2 (en) | 2020-12-29 | 2025-12-30 | Skyworks Solutions, Inc. | Low loss tangent dielectric based on spinel-structured oxide |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS605545B2 (en) * | 1980-03-19 | 1985-02-12 | 日本碍子株式会社 | Low expansion ceramics and their manufacturing method |
| JPS6021940B2 (en) * | 1980-12-08 | 1985-05-30 | 日立金属株式会社 | Non-magnetic ceramics for magnetic heads |
-
1984
- 1984-09-22 JP JP59199099A patent/JPS6177208A/en active Granted
-
1985
- 1985-09-23 US US06/778,652 patent/US4614725A/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6177208A (en) | 1986-04-19 |
| US4614725A (en) | 1986-09-30 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| LAPS | Cancellation because of no payment of annual fees |